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2027 Co-Op, PTE

Moderna

Norwood, MAHybridPosted 5 days ago$20.00 - $60.00/hour
InternshipInternProgram / Project ManagementBiotechnology
Original posting ↗

Summary

This is a co-op opportunity based in Norwood, MA from January 18, 2027 – June 25, 2027, and applicants must be available for the full duration of the co-op term.

Job description

As an individual contributor within Development Process, Training & Execution, you will help advance innovation and digital enablement initiatives that streamline workflows, improve access to information, and strengthen adoption of digital tools across Moderna’s Development organization.

Here’s What You’ll Do

  • Support innovation and digital enablement efforts by gathering user needs, documenting current-state workflows, testing proposed solutions, and preparing user guidance or training materials under team supervision.
  • Collaborate with cross-functional partners to explore practical uses of automation, dashboards, and approved AI-enabled tools for document management, knowledge sharing, and process efficiency, helping summarize findings and recommendations.
  • Gain exposure to approved Generative AI tools and help evaluate where they may support more efficient information access, knowledge sharing, documentation, and digital ways of working within appropriate Moderna frameworks.
  • Contribute to process mapping, workflow documentation, and continuous improvement projects, including identifying opportunities to simplify manual steps and enable more efficient digital processes.
  • Support the drafting, formatting, and revision of standard operating procedures (SOPs), work instructions (WIs), and related controlled documents using established templates and guidance.
  • Assist with quality control reviews of controlled documents for clarity, consistency, formatting, cross-references, and alignment with applicable document standards.
  • Help maintain and enhance document trackers, action logs, dashboards, and project status reports to support controlled document development, digital visibility, and implementation.
  • Assist with document lifecycle, training, and digital workflow activities in systems such as Veeva Quality, Smartsheet, and Microsoft 365 tools, as appropriate to assigned access and training.
  • Support the organization and analysis of process documentation, training matrices, and related records to identify gaps and opportunities for improvement.
  • Work closely with process, training, and cross-functional partners to support consistent execution and effective adoption of new or improved processes and digital tools across Development.
  • Build practical experience working within a regulated, quality-focused clinical development environment while contributing to projects that improve how teams access information, manage documentation, and execute work.

Here’s What You’ll Need (Basic Qualifications)

  • Currently enrolled in a Bachelor’s or Master’s degree program in Life Sciences, Business, Engineering, Quality, Healthcare Administration, or a related field.
  • Proficiency with Microsoft Office applications, particularly Word, Excel, and PowerPoint, and an interest in learning digital collaboration and workflow tools.
  • Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.

Here’s What You’ll Bring to the Table (Preferred Qualifications)

  • GPA of 3.5 (on a 4.0 scale) or equivalent academic achievement.
  • Strong organizational skills and ability to manage multiple assignments while working collaboratively with cross-functional teams.
  • Clear written and verbal communication skills, including an interest in technical writing and document editing.
  • High attention to detail, with an interest in process quality, consistency, and continuous improvement.
  • Curiosity about digital tools, workflow automation, data visualization, or responsible use of AI to improve business processes; prior experience is a plus but not required.
  • Interest in clinical development operations, regulated processes, quality systems, training, process improvement, innovation, or digital transformation.

Requirements

  • Currently enrolled in a Bachelor’s or Master’s degree program in Life Sciences, Business, Engineering, Quality, Healthcare Administration, or a related field.
  • Proficiency with Microsoft Office applications, particularly Word, Excel, and PowerPoint.
  • Interest in learning digital collaboration and workflow tools.
  • Candidates must already hold work authorization in US and be able to maintain that status without the need for future sponsorship.

Benefits

  • Meditation and mindfulness classes
  • Subsidized commuter benefits
  • Paid time off
  • Vacation
  • Sick time
  • Holidays
  • Volunteer days
  • Discretionary year-end shutdown
  • Location-specific perks

Company overview

Moderna, Inc. is a pioneering American biotechnology and pharmaceutical company headquartered in Cambridge, Massachusetts, that has revolutionized the field of medicine through its groundbreaking messenger RNA (mRNA) technology. Founded in 2010, the company has established itself as a global leader in RNA therapeutics, primarily focusing on mRNA vaccines and treatments. Moderna's innovative platform uses mRNA to provide cellular instructions for producing proteins that trigger immune responses, creating a new category of medicines with significant potential to improve patient outcomes across various therapeutic areas. The company gained worldwide recognition during the COVID-19 pandemic for developing one of the earliest and most effective mRNA vaccines, which demonstrated the transformative potential of its technology platform. Beyond infectious diseases, Moderna is advancing a diverse pipeline of 44 treatment and vaccine candidates across infectious diseases, immuno-oncology, rare diseases, cardiovascular diseases, and autoimmune conditions. With approximately 5,800 employees and a strong commitment to scientific innovation, Moderna continues to expand its manufacturing capabilities and research initiatives to deliver the greatest possible impact through mRNA medicines.

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